Naive B cells and somatically mutated memory cells are produced by a process involving cell proliferation accompanied by stringent cellular selection, so that only cells of the desired phenotype survive. In both processes there is positive selection, first of cells with an in frame VHDHJH rearrangement, which can thus express a p-chain in the pBCR; then of B cells expressing a complete antibody in a functional receptor complex, presumably through expression of the BCR; and finally of somatic mutants expressing high-affinity antibodies in their BCR in the germinal center reaction. Only in the last case do we know the ligand that drives the selection; at earlier stages, selection may be driven by ligands on cells in the environment or by cell-autonomous mechanisms. In all cases, however, unselected cells are rapidly lost from the system, presumably by apoptosis.
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Dr. Prakash K K is working as Associate Professor in the department of Biotechnology department in G M Institute of Technology, Davanagere, affiliated to VTU Belagavi and AICTE New Delhi. He obtained his Post Graduation from Kuvempu University, Shnakarghatta and Ph.D. from Visvesvaraya Technological University Belagavi.
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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Naive B cells and somatically mutated memory cells are produced by a process involving cell proliferation accompanied by stringent cellular selection, so that only cells of the desired phenotype survive. In both processes there is positive selection, first of cells with an in frame VHDHJH rearrangement, which can thus express a p-chain in the pBCR; then of B cells expressing a complete antibody in a functional receptor complex, presumably through expression of the BCR; and finally of somatic mutants expressing high-affinity antibodies in their BCR in the germinal center reaction. Only in the last case do we know the ligand that drives the selection; at earlier stages, selection may be driven by ligands on cells in the environment or by cell-autonomous mechanisms. In all cases, however, unselected cells are rapidly lost from the system, presumably by apoptosis. 60 pp. Englisch. Bestandsnummer des Verkäufers 9786202680219
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Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: K K PrakashDr. Prakash K K is working as Associate Professor in the department of Biotechnology department in G M Institute of Technology, Davanagere, affiliated to VTU Belagavi and AICTE New Delhi. He obtained his Post Graduation fr. Bestandsnummer des Verkäufers 494421910
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Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Naive B cells and somatically mutated memory cells are produced by a process involving cell proliferation accompanied by stringent cellular selection, so that only cells of the desired phenotype survive. In both processes there is positive selection, first of cells with an in frame VHDHJH rearrangement, which can thus express a p-chain in the pBCR; then of B cells expressing a complete antibody in a functional receptor complex, presumably through expression of the BCR; and finally of somatic mutants expressing high-affinity antibodies in their BCR in the germinal center reaction. Only in the last case do we know the ligand that drives the selection; at earlier stages, selection may be driven by ligands on cells in the environment or by cell-autonomous mechanisms. In all cases, however, unselected cells are rapidly lost from the system, presumably by apoptosis.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 60 pp. Englisch. Bestandsnummer des Verkäufers 9786202680219
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Naive B cells and somatically mutated memory cells are produced by a process involving cell proliferation accompanied by stringent cellular selection, so that only cells of the desired phenotype survive. In both processes there is positive selection, first of cells with an in frame VHDHJH rearrangement, which can thus express a p-chain in the pBCR; then of B cells expressing a complete antibody in a functional receptor complex, presumably through expression of the BCR; and finally of somatic mutants expressing high-affinity antibodies in their BCR in the germinal center reaction. Only in the last case do we know the ligand that drives the selection; at earlier stages, selection may be driven by ligands on cells in the environment or by cell-autonomous mechanisms. In all cases, however, unselected cells are rapidly lost from the system, presumably by apoptosis. Bestandsnummer des Verkäufers 9786202680219
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